ALBERT

Description: Large peridotite massifs are scattered along the 1500 km length of the Yarlung–Zangbo Suture Zone (southern Tibet, China), the major suture between Asia and Greater India. Diamonds occur in the peridotites and chromitites of several massifs, together with an extensive suite of trace phases that indicate extremely low f O 2 (SiC, nitrides, carbides, native elements) and/or ultrahigh pressures (UHP) (diamond, TiO 2 II, coesite, possible stishovite). New physical and isotopic (C, N) studies of the diamonds indicate that they are natural, crystallized in a disequilibrium, high- T environment, and spent only a short time at mantle temperatures before exhumation and cooling. These constraints are difficult to reconcile with previous models for the history of the diamond-bearing rocks. Possible evidence for metamorphism in or near the upper part of the Transition Zone includes the following: (1) chromite (in disseminated, nodular and massive chromitites) containing exsolved pyroxenes and coesite, suggesting inversion from a high- P polymorph of chromite; (2) microstructural studies suggesting that the chromitites recrystallized from fine-grained, highly deformed mixtures of wadsleyite and an octahedral polymorph of chromite; (3) a new cubic Mg-silicate, with the space group of ringwoodite but an inverse-spinel structure (all Si in octahedral coordination); (4) harzburgites with coarsely vermicular symplectites of opx + Cr–Al spinel ± cpx; reconstructions suggest that these are the breakdown products of majoritic garnets, with estimated minimum pressures to 〉 13 GPa. Evidence for a shallow pre-metamorphic origin for the chromitites and peridotites includes the following: (1) trace-element data showing that the chromitites are typical of suprasubduction-zone (SSZ) chromitites formed by magma mixing or mingling, consistent with Hf-isotope data from magmatic (375 Ma) zircons in the chromitites; (2) the composition of the new cubic Mg-silicate, which suggests a low- P origin as antigorite, subsequently dehydrated; (3) the peridotites themselves, which carry the trace element signature of metasomatism in an SSZ environment, a signature that must have been imposed before the incorporation of the UHP and low- f O 2 phases. A proposed P – T – t path involves the original formation of chromitites in mantle-wedge harzburgites, subduction of these harzburgites at c . 375 Ma, residence in the upper Transition Zone for 〉200 Myr, and rapid exhumation at c . 170–150 Ma or 130–120 Ma. Os-isotope data suggest that the subducted mantle consisted of previously depleted subcontinental lithosphere, dragged down by a subducting oceanic slab. Thermomechanical modeling shows that roll-back of a (much later) subducting slab would produce a high-velocity channelized upwelling that could exhume the buoyant harzburgites (and their chromitites) from the Transition Zone in 〈 10 Myr. This rapid upwelling, which may explain some characteristics of the diamonds, appears to have brought some massifs to the surface in forearc or back-arc basins, where they provided a basement for oceanic crust. This model can reconcile many apparently contradictory petrological and geological datasets. It also defines an important, previously unrecognized geodynamic process that may have operated along other large suture zones such as the Urals.

Description: Chromite from Los Congos and Los Guanacos in the Eastern Pampean Ranges of Córdoba (Argentinian Central Andes) shows homogenous and exsolution textures. The composition of the exsolved phases in chromite approaches the end-members of spinel (MgAl 2 O 4 ; Spl) and magnetite ( $${\mathrm{Fe}}^{2+}{\mathrm{Fe}}_{2}^{3+}{\mathrm{O}}_{4}$$ ; Mag) that define the corners of the spinel prism at relatively constant Cr 3+ /R 3+ ratio (where R 3+ is Cr+Al+Fe 3+ ). The exsolution of these phases from the original chromite is estimated to have accounted at ≥600 °C on the basis of the major element compositions of chromite with homogenous and exsolution textures that are in equilibrium with forsterite-rich olivine (Fo 95 ). The relatively large size of the exsolved phases in chromite (up to ca. 200 μm) provided, for the first time, the ability to conduct in situ analysis with laser ablation-inductively coupled plasma-mass spectrometry for a suite of minor and trace elements to constrain their crystal-crystal partition coefficient between the spinel-rich and magnetite-rich phases $$({D}_{\mathrm{i}}^{\mathrm{Spl}/\mathrm{Mag}})$$ . Minor and trace elements listed in increasing order of compatibility with the spinel-rich phase are Ti, Sc, Ni, V, Ge, Mn, Cu, Sn, Co, Ga, and Zn. $${D}_{\mathrm{i}}^{\mathrm{Spl}/\mathrm{Mag}}$$ values span more than an order of magnitude, from $${D}_{\mathrm{Ti}}^{\mathrm{Spl}/\mathrm{Mag}}=0.30\pm 0.06$$ to $${D}_{\mathrm{Zn}}^{\mathrm{Spl}/\mathrm{Mag}}=5.48\pm 0.63$$ . Our results are in remarkable agreement with data available for exsolutions of spinel-rich and magnetite-rich phases in other chromite from nature, despite their different Cr 3+ /R 3+ ratio. The estimated crystal-crystal partitioning coefficients reflect the effect that crystal-chemistry of the exsolved phases from chromite imposes on all investigated elements, excepting Cu and Sc (and only slightly for Mn). The observed preferential partitioning of Ti and Sc into the magnetite-rich phase is consistent with high-temperature chromite/melt experiments and suggests a significant dependence on Fe 3+ substitution in the spinel structure. A compositional effect of major elements on Ga, Co, and Zn is observed in the exsolved phases from chromite but not in the experiments; this might be due to crystal-chemistry differences along the $${\mathrm{MgFe}}_{-1}{-\mathrm{Al}}_{2}{\mathrm{Fe}}_{-2}^{3+}$$ exchange vector, which is poorly covered experimentally. This inference is supported by the strong covariance of Ga, Co, and Zn observed only in chromite from layered intrusions where this exchange vector is important. A systematic increase of Zn and Co coupled with a net decrease in Ga during hydrous metamorphism of chromitite bodies cannot be explained exclusively by compositional changes of major elements in the chromite (which are enriched in the magnetite component). The most likely explanation is that the contents of minor and trace elements in chromite from metamorphosed chromitites are controlled by interactions with metamorphic fluids involved in the formation of chlorite.

Description: We suggest a new explanation for the presence of crustally derived zircons in the upper-mantle rocks of ophiolitic complexes, as an alternative to subduction-related models. Integrated isotopic (U-Pb, Hf, and O isotopes) and trace-element data for zircons from the Tumut ophiolitic complex (southeast Australia) indicate that these grains are related to granitic magmatism and were introduced into the mantle rocks after their emplacement into the crust. These observations emphasize that a clear understanding of the origin of individual zircon populations and their relationship to the host rock is essential to interpretations of the tectonic history of upper-mantle rocks and the dynamics of crust-mantle interactions.

Description: Podiform chromitites enclosed in depleted harzburgites of the Luobusa massif (southeastern Tibet) contain diamond and a highly reduced trace-mineral association. Exsolution of diopside and coesite from chromite suggests inversion from the Ca-ferrite structure in the upper part of the mantle transition zone (〉400 km). However, the trace-element signatures of the chromites are typical of ophiolitic chromitites, implying primary crystallization at shallow depths. Os-Ir nuggets in the chromitites have Re-Os model ages ( T RD ) of 234 ± 3 Ma, while T RD ages of in situ Ru-Os-Ir sulfides range from 290 to 630 Ma, peaking at ca. 325 Ma. Euhedral zircons in the chromitites give U-Pb ages of 376 ± 7 Ma, Hf = 9.7 ± 4.6, and 18 O = 4.8–8.2. The sulfide and zircon ages may date formation of the chromitites from boninite-like melts in a supra-subduction-zone environment, while the model ages of Os-Ir nuggets may date local reduction in the transition zone following Devonian subduction. Thermo-mechanical modeling suggests a rapid (10 m.y.) rise of the buoyant harzburgites from 〉400 km depth during the early Tertiary and/or Late Cretaceous rollback of the Indian slab. This process may occur in other collision zones; mantle samples from the transition zone may be more widespread than currently recognized.

Description: Author(s): J. M. Pearson, N. Chamel, A. Pastore, and S. Goriely The TETFSI (temperature-dependent extended Thomas-Fermi plus Strutinsky integral) method for calculating the properties of the inner crust of neutron stars is here extended in the zero-temperature limit to include proton pairing. The main effect is to smooth out the proton shell effects, although th... [Phys. Rev. C 91, 018801] Published Wed Jan 14, 2015

Description: The minimum oxygen fugacity ( f O 2 ) of Earth’s upper mantle probably is controlled by metal saturation, as defined by the iron-wüstite (IW) buffer reaction (FeO -〉 Fe + O). However, the widespread occurrence of moissanite (SiC) in kimberlites, and a suite of super-reduced minerals (SiC, alloys, native elements) in peridotites in Tibet and the Polar Urals (Russia), suggest that more reducing conditions ( f O 2 = 6–8 log units below IW) must occur locally in the mantle. We describe pockets of melt trapped in aggregates of corundum crystals ejected from Cretaceous volcanoes in northern Israel which contain high-temperature mineral assemblages requiring extremely low f O 2 (IW 〈 –10). One abundant phase is tistarite (Ti 2 O 3 ), previously known as a single grain in the Allende carbonaceous chondrite (Mexico) and believed to have formed during the early evolution of the solar nebula. It is associated with other reduced phases usually found in meteorites. The development of super-reducing conditions in Earth’s upper mantle may reflect the introduction of CH 4 + H 2 fluids from the deep mantle, specifically related to deep-seated volcanic plumbing systems at plate boundaries.

Description: Ultrahigh-pressure ( UHP ) materials ( e.g ., diamond, high-pressure polymorph of chromite) and super-reduced (SuR) phases ( e.g ., carbides, nitrides, silicides and native metals) have been identified in chromitites and peridotites of the Tibetan and Polar-Urals ophiolites. These unusual assemblages suggest previously unrecognized fluid- or melt-related processes in the Earth’s mantle. However, the origin of the SuR phases, and in particular their relationships with the UHP materials in the ophiolites, are still enigmatic. Studies of a recently recognized SuR mineral system from Cretaceous volcanics on Mt Carmel, Israel, suggest an alternative genesis for the ophiolitic SuR phases. The Mt Carmel SuR mineral system (associated with Ti-rich corundum xenocrysts) appears to reflect the local interaction of mantle-derived CH 4 ± H 2 fluids with basaltic magmas in the shallow lithosphere (depths of ~30–100 km). These interactions produced desilication of the magma, supersaturation in Al 2 O 3 leading to rapid growth of corundum, and phase assemblages requiring local oxygen fugacity ( f O 2 ) gradually dropping to ~11 log units below the iron–wüstite (IW) buffer. The strong similarities between this system and the SuR phases and associated Ti-rich corundum in the Tibetan and Polar-Urals ophiolites suggest that the ophiolitic SuR suite probably formed by local influx of CH 4 ± H 2 fluids within previously subducted peridotites (and included chromitites) during their rapid exhumation from the deep upper mantle to lithospheric levels. In the final stages of their ascent, the recycled peridotites and chromitites were overprinted by a shallow magmatic system similar to that observed at Mt Carmel, producing most of the SuR phases and eventually preserving them within the Tibetan and Polar-Urals ophiolites.

Description: The minimum oxygen fugacity ( f O 2 ) of Earth’s upper mantle probably is controlled by metal saturation, as defined by the iron-wüstite (IW) buffer reaction (FeO -〉 Fe + O). However, the widespread occurrence of moissanite (SiC) in kimberlites, and a suite of super-reduced minerals (SiC, alloys, native elements) in peridotites in Tibet and the Polar Urals (Russia), suggest that more reducing conditions ( f O 2 = 6–8 log units below IW) must occur locally in the mantle. We describe pockets of melt trapped in aggregates of corundum crystals ejected from Cretaceous volcanoes in northern Israel which contain high-temperature mineral assemblages requiring extremely low f O 2 (IW 〈 –10). One abundant phase is tistarite (Ti 2 O 3 ), previously known as a single grain in the Allende carbonaceous chondrite (Mexico) and believed to have formed during the early evolution of the solar nebula. It is associated with other reduced phases usually found in meteorites. The development of super-reducing conditions in Earth’s upper mantle may reflect the introduction of CH 4 + H 2 fluids from the deep mantle, specifically related to deep-seated volcanic plumbing systems at plate boundaries.